drugset / Trial / NCT01960686

RSV F Dose-Ranging Study in Women

NCT01960686

Phase 2 Completed 720 enrolled Novavax
RandomizedParallel-groupTriple-blindTreatment

Summary

The purpose of this study is to evaluate the immunogenicity and safety of multiple formulations of an RSV-F protein nanoparticle vaccine, with aluminum, in healthy women of child-bearing age.

Timeline

Start
2013-10
Primary completion
2014-04
Completion
2014-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Aluminum Phosphate Unknown 0.2 mg Intramuscular
Subject Aluminum Phosphate Unknown 0.4 mg Intramuscular
Subject Aluminum Phosphate Unknown 0.8 mg Intramuscular
Subject RSV F protein Vaccine 60 ug Intramuscular
Subject RSV F protein Vaccine 120 ug Intramuscular